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Amiloride Hydrochloride
Amiloride Hydrochloride - 49884-117-10 - (Amiloride Hydrochloride)
Drug Information of Amiloride Hydrochloride
| Product NDC: | 49884-117 |
| Proprietary Name: | Amiloride Hydrochloride |
| Non Proprietary Name: | Amiloride Hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Amiloride Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amiloride Hydrochloride
| Product NDC: | 49884-117 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070346 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19860122 |
Package Information of Amiloride Hydrochloride
| Package NDC: | 49884-117-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (49884-117-10) |
NDC Information of Amiloride Hydrochloride
| NDC Code | 49884-117-10 |
| Proprietary Name | Amiloride Hydrochloride |
| Package Description | 1000 TABLET in 1 BOTTLE (49884-117-10) |
| Product NDC | 49884-117 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amiloride Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19860122 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | AMILORIDE HYDROCHLORIDE ANHYDROUS |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
